Class II medical devices recalls – page 8

• M5 Corpus Power Wheelchair recall
  FDA August 5, 2026 · Permobil Inc · Class II
• L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm recall
  FDA August 5, 2026 · Argon Medical Devices, Inc · Class II
• L-Cath PICC S/L Peripherally Inserted Central Catheter: 26ga (1.9F) 0.60mm… recall
  FDA August 5, 2026 · Argon Medical Devices, Inc · Class II
• AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1)… recall
  FDA August 5, 2026 · Windstone Medical Packaging, Inc. · Class II
• AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1)… recall
  FDA August 5, 2026 · Windstone Medical Packaging, Inc. · Class II
• AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) ENT… recall
  FDA August 5, 2026 · Windstone Medical Packaging, Inc. · Class II
• AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) ENT… recall
  FDA August 5, 2026 · Windstone Medical Packaging, Inc. · Class II
• Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock recall
  FDA August 5, 2026 · Permobil Inc · Class II
• Power Over Fiber Base Module recall
  FDA August 5, 2026 · Terex Utilities · Class II
• Ingenuity CT CT5000 Ingenuity Plus CT5000 Ingenuity Pro CT5000 Ingenuity… recall
  FDA August 5, 2026 · Philips Medical Systems · Class II
• IQon Spectral CT IQon Spectral CT Upgrades recall
  FDA August 5, 2026 · Philips Medical Systems · Class II
• Brilliance iCT Brilliance iCT Upgrades Brilliance iCT SP Brilliance CT 64… recall
  FDA August 5, 2026 · Philips Medical Systems · Class II
• Flexible Hystero-Fiberscope Kits recall
  FDA July 29, 2026 · Karl Storz Endoscopy · Class II
• SafeOp Patient Interface recall
  FDA July 29, 2026 · Alphatec Spine, Inc. · Class II
• Medline medical convenience kits labeled as: 1) TOTAL JOINT PACK Medline… recall
  FDA July 29, 2026 · Medline Industries, LP · Class II
• Medline medical convenience kits labeled as: NEURO PACK… recall
  FDA July 29, 2026 · Medline Industries, LP · Class II
• Medline medical convenience kits labeled as: 1) SHOULDER PACK… recall
  FDA July 29, 2026 · Medline Industries, LP · Class II
• Medline medical convenience kits labeled as: 1) KIT PEDIATRIC OPEN HEART… recall
  FDA July 29, 2026 · Medline Industries, LP · Class II
• Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters… recall
  FDA July 29, 2026 · Medline Industries, LP · Class II
• Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters… recall
  FDA July 29, 2026 · Medline Industries, LP · Class II
• Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters… recall
  FDA July 29, 2026 · Medline Industries, LP · Class II
• Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters… recall
  FDA July 29, 2026 · Medline Industries, LP · Class II
• Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters… recall
  FDA July 29, 2026 · Medline Industries, LP · Class II
• Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters… recall
  FDA July 29, 2026 · Medline Industries, LP · Class II
• Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters… recall
  FDA July 29, 2026 · Medline Industries, LP · Class II
• Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters… recall
  FDA July 29, 2026 · Medline Industries, LP · Class II
• Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters… recall
  FDA July 29, 2026 · Medline Industries, LP · Class II
• MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android) recall
  FDA July 29, 2026 · Medtronic MiniMed, Inc. · Class II
• Emano Flow with software version v2.0.0 GS1 GTIN code: 199874903484 Emano… recall
  FDA July 29, 2026 · Emano Metrics, Inc. · Class II
• Olympus High Flow Insufflation Unit - UHI-4. Model Number: UHI-4 recall
  FDA July 29, 2026 · Olympus Corporation of the Americas · Class II
• SnapshotGLO Wound Imaging Device, Model KB100, KB100AA recall
  FDA July 29, 2026 · Kent Imaging, Inc. · Class II
• Pipeline Flex Embolization Device with Shield Technology… recall
  FDA July 29, 2026 · Micro Therapeutics, Inc. · Class II
• Pipeline Flex Embolization Device with Shield Technology… recall
  FDA July 29, 2026 · Micro Therapeutics, Inc. · Class II
• Halyard STANDARD LINE INSERTION PACK. Model recall
  FDA July 29, 2026 · AVID Medical, Inc. · Class II
• Boston Scientific TheraSphere 360 Y-90 Management Platform… recall
  FDA July 29, 2026 · Boston Scientific Corporation · Class II
• Penumbra System RED 68 Reperfusion Catheter recall
  FDA July 29, 2026 · Penumbra, Inc. · Class II
• Silent Nite Product Name: Silent Nite Sleep Appliance Model recall
  FDA July 29, 2026 · Prismatik Dentalcraft, Inc. · Class II
• Ventriculostomy Kit recall
  FDA July 29, 2026 · Medtronic Neurosurgery · Class II
• 3mensio Workstation (Vascular Fenestrated) software recall
  FDA July 29, 2026 · PIE Medical Imaging B.V. · Class II
• Halyard EYE PACK. Model recall
  FDA July 29, 2026 · AVID Medical, Inc. · Class II
• SeaSpine Polyaxial Head recall
  FDA July 29, 2026 · Seaspine Orthopedics Corporation · Class II
• Olympus 4K UHD LCD Monitor recall
  FDA July 29, 2026 · Olympus Corporation of the Americas · Class II
• Power F2 Powered Fastening System, Product No recall
  FDA July 29, 2026 · Ferno-Washington Inc · Class II
• Hotline Fluid Warming Set, single use device… recall
  FDA July 29, 2026 · ICU Medical, Inc. · Class II
• P28 PHANTON INTRAMEDULLARY NAIL SYSTEM, Phantom Hindfoot TTC/TC Ball… recall
  FDA July 29, 2026 · Paragon 28, Inc. · Class II
• FARADRIVE STEERABLE SHEATH CLEAR OUS, used to facilitate access to the… recall
  FDA July 29, 2026 · Boston Scientific Corporation · Class II
• FARADRIVE STEERABLE SHEATH (CLEAR) - US, used to facilitate access to the… recall
  FDA July 29, 2026 · Boston Scientific Corporation · Class II
• FARADRIVE STEERABLE SHEATH CLEAR, used to facilitate access to the… recall
  FDA July 29, 2026 · Boston Scientific Corporation · Class II
• FARADRIVE Steerable Sheath Clear IDE, used to facilitate access to the… recall
  FDA July 29, 2026 · Boston Scientific Corporation · Class II
• FARASTAR Ablation Generator EU, Pulsed Field Ablation Generator… recall
  FDA July 29, 2026 · Boston Scientific Corporation · Class II
• FARASTAR PFA Generator, Product ID M004PFCE61M460 recall
  FDA July 29, 2026 · Boston Scientific Corporation · Class II
• FARASTAR Pulsed Field Ablation Generator, Product ID M004PFCE61M401 recall
  FDA July 29, 2026 · Boston Scientific Corporation · Class II
• FARASTAR Ablation Generator EU, Pulsed Field Ablation Generator… recall
  FDA July 29, 2026 · Boston Scientific Corporation · Class II
• The intended use is to be paired with a weapon for aiming purposes recall
  FDA July 29, 2026 · Wilcox Industries Corp. · Class II
• ST AIA-Pack Testosterone, IN VITRO DIAGNOSTIC USE ONLY for the… recall
  FDA July 22, 2026 · Tosoh Bioscience Inc · Class II
• Photera 600 3-D, phototherapy device recall
  FDA July 22, 2026 · Daavlin Distributing Company · Class II
• Photera 600, phototherapy device recall
  FDA July 22, 2026 · Daavlin Distributing Company · Class II
• Photera 400, phototherapy device recall
  FDA July 22, 2026 · Daavlin Distributing Company · Class II
• The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System (Model VH-4000 recall
  FDA July 22, 2026 · Maquet Cardiovascular, LLC · Class II
• Rio" II Product Name: Rio" II Nasal Pillows Interface Model recall
  FDA July 22, 2026 · 3B Medical, Inc. · Class II